Department of Oncology in First Affiliated Hospital of Hebei North University, Zhangjiakou, China.
Laboratory of the First Affiliated Hospital of University of Science and Technology of China, China.
Cell Biochem Funct. 2018 Jul;36(5):255-262. doi: 10.1002/cbf.3337. Epub 2018 Jun 3.
Human non-small cell lung cancer (NSCLC) is one of the leading causes of cancer deaths worldwide. Estrogenic signals have been suggested to be important for the growth and metastasis of NSCLC cells. Our present data showed that estrogen-related receptor alpha (ERRα), while not ERRβ or ERRγ, was significantly elevated in NSCLC cell lines as compared with that in normal bronchial epithelial cell line BEAS-2B. The expression of ERRα in clinical NSCLC tissues was significantly greater than that in their matched normal adjacent tissues. Over expression of ERRα can trigger the proliferation, migration, and invasion of NSCLC cells, while si-ERRα or ERRα inhibitor showed opposite effects. ERRα can increase the mRNA and protein expression of IL-6, while not IL-8, IL-10, IL-22, VEGF, TGF-β, or TNF-α, in NSCLC cells. Silence of IL-6 attenuated ERRα induced proliferation and cell invasion. Furthermore, our data revealed the inhibition of NF-κB, while not ERK1/2 or PI3K/Akt, abolished ERRα induced production of IL-6. This might be due to that overexpression of ERRα can increase the expression and nuclear translocation of p65 in NSCLC cells. Collectively, our data showed that activation of NF-κB/IL-6 is involved in ERRα induced migration and invasion of NSCLC cells. It suggested that ERRα might be a potential target for NSCLC treatment.
人非小细胞肺癌(NSCLC)是全球癌症死亡的主要原因之一。雌激素信号被认为对 NSCLC 细胞的生长和转移很重要。我们目前的数据表明,雌激素相关受体α(ERRα),而不是 ERRβ或 ERRγ,在 NSCLC 细胞系中明显高于正常支气管上皮细胞系 BEAS-2B。临床 NSCLC 组织中 ERRα的表达明显高于其配对的正常相邻组织。ERRα的过表达可引发 NSCLC 细胞的增殖、迁移和侵袭,而 si-ERRα 或 ERRα 抑制剂则表现出相反的效果。ERRα可增加 NSCLC 细胞中 IL-6 的 mRNA 和蛋白表达,而不增加 IL-8、IL-10、IL-22、VEGF、TGF-β 或 TNF-α的表达。IL-6 的沉默减弱了 ERRα诱导的增殖和细胞侵袭。此外,我们的数据还揭示了 NF-κB 的抑制作用,而不是 ERK1/2 或 PI3K/Akt,消除了 ERRα诱导的 IL-6 产生。这可能是因为 ERRα的过表达可以增加 NSCLC 细胞中 p65 的表达和核转位。总之,我们的数据表明,NF-κB/IL-6 的激活参与了 ERRα诱导的 NSCLC 细胞迁移和侵袭。这表明 ERRα可能是 NSCLC 治疗的一个潜在靶点。